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A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System
Microbes typically exist in mixed communities and display complex synergistic and antagonistic interactions. The Type VI secretion system (T6SS) is widespread in Gram-negative bacteria and represents a contractile nano-machine that can fire effector proteins directly into neighbouring cells. The pri...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617251/ https://www.ncbi.nlm.nih.gov/pubmed/31197124 http://dx.doi.org/10.3390/jof5020050 |
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author | Trunk, Katharina Coulthurst, Sarah J. Quinn, Janet |
author_facet | Trunk, Katharina Coulthurst, Sarah J. Quinn, Janet |
author_sort | Trunk, Katharina |
collection | PubMed |
description | Microbes typically exist in mixed communities and display complex synergistic and antagonistic interactions. The Type VI secretion system (T6SS) is widespread in Gram-negative bacteria and represents a contractile nano-machine that can fire effector proteins directly into neighbouring cells. The primary role assigned to the T6SS is to function as a potent weapon during inter-bacterial competition, delivering antibacterial effectors into rival bacterial cells. However, it has recently emerged that the T6SS can also be used as a powerful weapon against fungal competitors, and the first fungal-specific T6SS effector proteins, Tfe1 and Tfe2, have been identified. These effectors act via distinct mechanisms against a variety of fungal species to cause cell death. Tfe1 intoxication triggers plasma membrane depolarisation, whilst Tfe2 disrupts nutrient uptake and induces autophagy. Based on the frequent coexistence of bacteria and fungi in microbial communities, we propose that T6SS-dependent antifungal activity is likely to be widespread and elicited by a suite of antifungal effectors. Supporting this hypothesis, homologues of Tfe1 and Tfe2 are found in other bacterial species, and a number of T6SS-elaborating species have been demonstrated to interact with fungi. Thus, we envisage that antifungal T6SS will shape many polymicrobial communities, including the human microbiota and disease-causing infections. |
format | Online Article Text |
id | pubmed-6617251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66172512019-07-18 A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System Trunk, Katharina Coulthurst, Sarah J. Quinn, Janet J Fungi (Basel) Review Microbes typically exist in mixed communities and display complex synergistic and antagonistic interactions. The Type VI secretion system (T6SS) is widespread in Gram-negative bacteria and represents a contractile nano-machine that can fire effector proteins directly into neighbouring cells. The primary role assigned to the T6SS is to function as a potent weapon during inter-bacterial competition, delivering antibacterial effectors into rival bacterial cells. However, it has recently emerged that the T6SS can also be used as a powerful weapon against fungal competitors, and the first fungal-specific T6SS effector proteins, Tfe1 and Tfe2, have been identified. These effectors act via distinct mechanisms against a variety of fungal species to cause cell death. Tfe1 intoxication triggers plasma membrane depolarisation, whilst Tfe2 disrupts nutrient uptake and induces autophagy. Based on the frequent coexistence of bacteria and fungi in microbial communities, we propose that T6SS-dependent antifungal activity is likely to be widespread and elicited by a suite of antifungal effectors. Supporting this hypothesis, homologues of Tfe1 and Tfe2 are found in other bacterial species, and a number of T6SS-elaborating species have been demonstrated to interact with fungi. Thus, we envisage that antifungal T6SS will shape many polymicrobial communities, including the human microbiota and disease-causing infections. MDPI 2019-06-14 /pmc/articles/PMC6617251/ /pubmed/31197124 http://dx.doi.org/10.3390/jof5020050 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Trunk, Katharina Coulthurst, Sarah J. Quinn, Janet A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title | A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title_full | A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title_fullStr | A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title_full_unstemmed | A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title_short | A New Front in Microbial Warfare—Delivery of Antifungal Effectors by the Type VI Secretion System |
title_sort | new front in microbial warfare—delivery of antifungal effectors by the type vi secretion system |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617251/ https://www.ncbi.nlm.nih.gov/pubmed/31197124 http://dx.doi.org/10.3390/jof5020050 |
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